Edwards Lifesciences Corp

Principal Engineer, NPD, Advanced Innovation and Technology

Edwards Lifesciences Corp$121K — $171K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's, Master's, or Ph.D. in Engineering or related field, with relevant industry experience (2-6 years).
  • Deep expertise in developing manufacturing technologies for complex devices.
  • Proficient in CAD software, including GD&T principles, for designing and troubleshooting.
  • Experience in tech transfer across geographies, including knowledge transfer kits.
  • Familiarity with design controls for Class II and III medical devices, especially catheter-based systems.

Responsibilities

  • Provide technical ownership of manufacturing technology development from EHU through all phases of the Product Development Process.
  • Champion process excellence and compliance with cGMP and EH&S standards during validations.
  • Collaborate closely with cross-functional teams to align on goals and drive actionable outcomes.
  • Identify manufacturing risks related to technology, materials, and design, and develop effective mitigations.
  • Lead development and implementation of problem-solving methodologies to improve operational outcomes.

Benefits

  • Competitive salary and performance-based incentives.
  • Various benefits programs tailored to the needs of employees and their families.
Full Job Description
How you'll make an impact:
  • Provide technical ownership for successful development of manufacturing technologies (processes) to seamlessly transition from Early Human Use (EHU) through all phases of Edwards' Product Development Process (PDP) to meet the manufacturing and supply chain needs of the Business Unit.
  • Champion design for manufacturability, design and process excellence, six sigma thinking, LEAN, cGMP, EH&S requirements in executing process validations.
  • Drive resource maximization while minimizing development expenditure.
  • Work in close collaboration with cross functional partners and peers from Pilot Ops and extended GSC functions such as sourcing, supplier development, supplier quality etc., BU functions such as R&D, PMO, Design Assurance (DA), Regulatory, to align on goals and drive action to meet commitments to the BU including product builds for R&D evaluation, clinical studies, and downstream needs as assigned.
  • Identify risks across manufacturing operations including those associated with or arising from technology, materials, skills/competencies, design requirements etc. and develop/implement mitigations to deliver successful outcomes for the business.
  • Lead the development and implementation of tools/methodologies for effective problem-solving, failure analysis, root cause investigation and best practices for agile deployment of responses and robust solutions that deliver superior results that also elevate learning, critical thinking, and impact across the business.
  • Drive build strategy, prioritization, and technical support for QST, pre DV, DV, OQ and PQ - Key Partner to Pilot on root cause investigations for manufacturing processes.
  • Ensure development and implementation of robust characterization and validation activities in collaboration with partners from R&D and quality, including deployment of critical control points (CCPs) in manufacturing.
  • Prioritize the timely development of critical to quality (CTQ) design elements and cascading CTQs to design inputs / outputs and establishing process controls / limits.
  • Oversee the design and development of manufacturing tools, fixtures and equipment that provide the highest levels of quality and mistake proofing while meeting or exceeding requirements for reliability and robustness that meet Edwards' standards for tools and fixtures including EH&S and ergonomic standards.


What you'll need (Required):
  • Bachelor's Degree in Engineering or Scientific field with 6 years of previously related industry experience OR
  • Master's Degree in Engineering or Scientific field with 5 years of previously related industry experience OR
  • Ph.D. in Engineering or Scientific Field with 2 years of previous related industry experience


What else we look for (Preferred):
  • Deep expertise in conceptualizing, designing, developing and successful implementation of manufacturing technologies for the assembly of complex devices.
  • Comfort with CAD package and self-reliant on CAD usage for medium to high-complexity designs including GD&T principles. Ability to review and trouble shoot engineering/component and assembly drawings, assess tolerancing and stack-ups, and application of industry standards such as ISO.
  • Track record with developing highly capable, reliable and scalable technologies that are agile.
  • Experience transferring manufacturing lines across sites/geographies and preparing tech transfer knowledge kit.
  • Knowledge of design controls for Class II & III medical devices, including familiarity with: catheter-based delivery system. implantable devices - NiTi, CoCr, and mechanical devices, polymeric materials, textiles, fabrics, etc. and associated technologies to inspect, join, attach, fabricate and integrate dissimilar materials.
  • Strong collaborator and communicator with a high degree of emotional intelligence and the ability to understand business partner needs and manage expectations.
  • Experience in preparing for and presenting project status to leadership, including the development, and managing of dashboards.
  • Sound understanding of engineering procedures while addressing issues with impact beyond own team based on knowledge of related disciplines.
  • Ability to influence cross-functional partners, business units, and/or sites and interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization.


Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California (CA), the base pay range for this position is $121,000 to $171,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

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